应产妇要求剖宫产。

Meera Viswanathan, Anthony G Visco, Katherine Hartmann, Mary Ellen Wechter, Gerald Gartlehner, Jennifer M Wu, Rachel Palmieri, Michele Jonsson Funk, Linda Lux, Tammeka Swinson, Kathleen N Lohr
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引用次数: 0

摘要

目的:RTI国际-北卡罗来纳大学教堂山分校循证实践中心(RTI- unc EPC)系统回顾了美国和其他发达国家剖宫产(CD)的趋势和发生率,产妇要求剖宫产(CDMR)与计划阴道分娩(PVD)的母婴结局,影响CDMR利弊程度的因素,以及未来的研究方向。数据来源:我们检索了MEDLINE、Cochrane协作资源和Embase,并确定了1406篇文章来对照先验纳入标准进行检查。我们纳入了从1990年至今发表的英文研究。研究必须包括关键参照组(CDMR或代理)和PVD之间的比较。综述方法:主要审稿人从纳入的文章中提取关键变量的详细数据;另一位资深审稿人证实了其准确性。结果:我们确定了13篇关于CD趋势和发病率的文章,54篇关于母婴结局的文章,5篇关于CDMR修饰因子的文章。CDMR的发病率似乎在增加。然而,准确评估其真实发病率或随时间变化的趋势是困难的,因为目前CDMR既不是一个公认的临床实体,也不是诊断编码或报销的准确报告指征。实际上没有关于CDMR的研究,因此知识库主要依赖于具有独特和显着局限性的代理的间接证据。此外,大多数研究通过实际交付路线比较结果,导致其与计划交付路线的相关性存在很大的不确定性。原发性CDMR和计划阴道分娩对于母亲或婴儿的个体结果可能确实不同。然而,我们对许多不同结果的综合评估表明,原发性CDMR和计划阴道分娩之间没有重大差异,但证据太弱,无法明确地得出完全没有差异的结论。鉴于现有数据有限,我们无法得出可能影响计划CDMR与PVD结果的因素的明确结论。结论:由于其与原发性CDMR的相关性很小,证据明显有限。未来的研究需要对交付路线和结果的术语达成共识;创建关于CDMR信息的最小数据集;改进研究设计和统计分析;关注重大成果及其特殊衡量问题;用更好的衡量策略评估短期和长期结果;更好地处理混杂因素;考虑不同结果的价值或效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cesarean delivery on maternal request.

Objectives: The RTI International-University of North Carolina at Chapel Hill Evidence-based Practice Center (RTI-UNC EPC) systematically reviewed the evidence on the trend and incidence of cesarean delivery (CD) in the United States and in other developed countries, maternal and infant outcomes of cesarean delivery on maternal request (CDMR) compared with planned vaginal delivery (PVD), factors affecting the magnitude of the benefits and harms of CDMR, and future research directions.

Data sources: We searched MEDLINE, Cochrane Collaboration resources, and Embase and identified 1,406 articles to examine against a priori inclusion criteria. We included studies published from 1990 to the present, written in English. Studies had to include comparison between the key reference group (CDMR or proxies) and PVD.

Review methods: A primary reviewer abstracted detailed data on key variables from included articles; a second senior reviewer confirmed accuracy.

Results: We identified 13 articles for trends and incidence of CD, 54 for maternal and infant outcomes, and 5 on modifiers of CDMR. The incidence of CDMR appears to be increasing. However, accurately assessing either its true incidence or trends over time is difficult because currently CDMR is neither a well-recognized clinical entity nor an accurately reported indication for diagnostic coding or reimbursement. Virtually no studies exist on CDMR, so the knowledge base rests chiefly on indirect evidence from proxies possessing unique and significant limitations. Furthermore, most studies compared outcomes by actual routes of delivery, resulting in great uncertainty as to their relevance to planned routes of delivery. Primary CDMR and planned vaginal delivery likely do differ with respect to individual outcomes for either mothers or infants. However, our comprehensive assessment, across many different outcomes, suggests that no major differences exist between primary CDMR and planned vaginal delivery, but the evidence is too weak to conclude definitively that differences are completely absent. Given the limited data available, we cannot draw definitive conclusions about factors that might influence outcomes of planned CDMR versus PVD.

Conclusions: The evidence is significantly limited by its minimal relevance to primary CDMR. Future research requires developing consensus about terminology for both delivery routes and outcomes; creating a minimum data set of information about CDMR; improving study design and statistical analyses; attending to major outcomes and their special measurement issues; assessing both short- and long-term outcomes with better measurement strategies; dealing better with confounders; and considering the value or utility of different outcomes.

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